NO131082B - - Google Patents
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- Publication number
- NO131082B NO131082B NO04831/72A NO483172A NO131082B NO 131082 B NO131082 B NO 131082B NO 04831/72 A NO04831/72 A NO 04831/72A NO 483172 A NO483172 A NO 483172A NO 131082 B NO131082 B NO 131082B
- Authority
- NO
- Norway
- Prior art keywords
- oxime
- aliphatic
- range
- sec
- general formula
- Prior art date
Links
- PXHVJJICTQNCMI-UHFFFAOYSA-N nickel Substances [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims description 49
- 125000001424 substituent group Chemical group 0.000 claims description 30
- 239000012074 organic phase Substances 0.000 claims description 25
- 238000000034 method Methods 0.000 claims description 20
- QGZKDVFQNNGYKY-UHFFFAOYSA-N ammonia Natural products N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 claims description 18
- 125000004432 carbon atom Chemical group C* 0.000 claims description 18
- 239000012071 phase Substances 0.000 claims description 14
- 239000000203 mixture Substances 0.000 claims description 13
- 229910052759 nickel Inorganic materials 0.000 claims description 13
- 125000001931 aliphatic group Chemical group 0.000 claims description 12
- 150000002923 oximes Chemical class 0.000 claims description 12
- 229910001868 water Inorganic materials 0.000 claims description 12
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 claims description 11
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 10
- 125000001183 hydrocarbyl group Chemical group 0.000 claims description 9
- 239000008346 aqueous phase Substances 0.000 claims description 8
- LZLWAYGVKBEDQT-UHFFFAOYSA-N 2-(N-hydroxy-C-phenylcarbonimidoyl)-4-nonan-2-ylphenol Chemical compound OC1=C(C(C2=CC=CC=C2)=NO)C=C(C=C1)C(CCCCCCC)C LZLWAYGVKBEDQT-UHFFFAOYSA-N 0.000 claims description 7
- HZXQKZWVTDAZAE-UHFFFAOYSA-N 2-(N-hydroxy-C-phenylcarbonimidoyl)phenol Chemical compound C=1C=CC=C(O)C=1C(=NO)C1=CC=CC=C1 HZXQKZWVTDAZAE-UHFFFAOYSA-N 0.000 claims description 7
- SLCANKHLTWZHRV-BMRADRMJSA-N (7e)-5,8-diethyl-7-hydroxyiminododecan-6-ol Chemical compound CCCCC(CC)C(O)C(=N\O)\C(CC)CCCC SLCANKHLTWZHRV-BMRADRMJSA-N 0.000 claims description 5
- 238000000622 liquid--liquid extraction Methods 0.000 claims description 4
- 238000000638 solvent extraction Methods 0.000 claims description 4
- 125000003545 alkoxy group Chemical group 0.000 claims description 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 3
- 239000003960 organic solvent Substances 0.000 claims description 3
- -1 copper Chemical class 0.000 description 31
- 239000000243 solution Substances 0.000 description 20
- 238000000605 extraction Methods 0.000 description 16
- 125000000217 alkyl group Chemical group 0.000 description 14
- 238000003756 stirring Methods 0.000 description 11
- 235000011114 ammonium hydroxide Nutrition 0.000 description 9
- 150000001875 compounds Chemical class 0.000 description 9
- 229910017052 cobalt Inorganic materials 0.000 description 8
- 239000010941 cobalt Substances 0.000 description 8
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 8
- 238000000926 separation method Methods 0.000 description 7
- 125000003342 alkenyl group Chemical group 0.000 description 6
- 239000012736 aqueous medium Substances 0.000 description 6
- 239000007864 aqueous solution Substances 0.000 description 6
- XLJKHNWPARRRJB-UHFFFAOYSA-N cobalt(2+) Chemical compound [Co+2] XLJKHNWPARRRJB-UHFFFAOYSA-N 0.000 description 6
- 229910052801 chlorine Inorganic materials 0.000 description 5
- 239000010410 layer Substances 0.000 description 5
- 238000011068 loading method Methods 0.000 description 5
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 4
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 4
- 125000004453 alkoxycarbonyl group Chemical group 0.000 description 4
- 239000000460 chlorine Substances 0.000 description 4
- 239000003350 kerosene Substances 0.000 description 4
- 229910052751 metal Inorganic materials 0.000 description 4
- 239000002184 metal Substances 0.000 description 4
- 239000012044 organic layer Substances 0.000 description 4
- 238000011084 recovery Methods 0.000 description 4
- 150000003839 salts Chemical class 0.000 description 4
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 229910021529 ammonia Inorganic materials 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 229910052802 copper Inorganic materials 0.000 description 3
- 239000010949 copper Substances 0.000 description 3
- 125000003493 decenyl group Chemical group [H]C([*])=C([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 3
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 3
- 238000002474 experimental method Methods 0.000 description 3
- 125000005842 heteroatom Chemical group 0.000 description 3
- 238000002386 leaching Methods 0.000 description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 3
- 125000005064 octadecenyl group Chemical group C(=CCCCCCCCCCCCCCCCC)* 0.000 description 3
- 125000004365 octenyl group Chemical group C(=CCCCCCC)* 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonium chloride Substances [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 2
- BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical compound OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 description 2
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 125000003710 aryl alkyl group Chemical group 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 2
- 229910052794 bromium Inorganic materials 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 125000005066 dodecenyl group Chemical group C(=CCCCCCCCCCC)* 0.000 description 2
- 238000005868 electrolysis reaction Methods 0.000 description 2
- 125000003754 ethoxycarbonyl group Chemical group C(=O)(OCC)* 0.000 description 2
- 238000001704 evaporation Methods 0.000 description 2
- 230000008020 evaporation Effects 0.000 description 2
- 125000005843 halogen group Chemical group 0.000 description 2
- 229930195733 hydrocarbon Natural products 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 239000002609 medium Substances 0.000 description 2
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 2
- 239000007800 oxidant agent Substances 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 125000002255 pentenyl group Chemical group C(=CCCC)* 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 2
- DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 description 1
- WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 description 1
- KNKRKFALVUDBJE-UHFFFAOYSA-N 1,2-dichloropropane Chemical compound CC(Cl)CCl KNKRKFALVUDBJE-UHFFFAOYSA-N 0.000 description 1
- 125000006219 1-ethylpentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C([H])([H])[H] 0.000 description 1
- NLCNYFGASBXHGN-UHFFFAOYSA-N 19-hydroxyiminohexatriaconta-9,27-dien-18-ol Chemical compound CCCCCCCCC=CCCCCCCCC(O)C(=NO)CCCCCCCC=CCCCCCCCC NLCNYFGASBXHGN-UHFFFAOYSA-N 0.000 description 1
- HYRJBVHCVUSFEO-UHFFFAOYSA-N 2-(C-heptadecyl-N-hydroxycarbonimidoyl)-4-octan-2-ylphenol Chemical compound OC1=C(C=C(C=C1)C(C)CCCCCC)C(CCCCCCCCCCCCCCCCC)=NO HYRJBVHCVUSFEO-UHFFFAOYSA-N 0.000 description 1
- VGIKRXWHMNSQAW-UHFFFAOYSA-N 2-(N-hydroxy-C-octylcarbonimidoyl)-4-octan-2-ylphenol Chemical compound C(CCCCCCC)C(C1=C(C=CC(=C1)C(C)CCCCCC)O)=NO VGIKRXWHMNSQAW-UHFFFAOYSA-N 0.000 description 1
- AKBZKVZFBPWCDC-UHFFFAOYSA-N 2-(N-hydroxy-C-pentylcarbonimidoyl)-4-undecan-2-ylphenol Chemical compound C(CCCC)C(C1=C(C=CC(=C1)C(C)CCCCCCCCC)O)=NO AKBZKVZFBPWCDC-UHFFFAOYSA-N 0.000 description 1
- MGGMLMZGRSINMD-UHFFFAOYSA-N 2-(N-hydroxy-C-tridecylcarbonimidoyl)-4-methylphenol Chemical compound C(CCCCCCCCCCCC)C(C1=C(C=CC(=C1)C)O)=NO MGGMLMZGRSINMD-UHFFFAOYSA-N 0.000 description 1
- JTYQYQHFAQIVQX-UHFFFAOYSA-N 2-(N-hydroxy-C-undecylcarbonimidoyl)-4-octan-2-ylphenol Chemical compound C(CCCCCCCCCC)C(C1=C(C=CC(=C1)C(C)CCCCCC)O)=NO JTYQYQHFAQIVQX-UHFFFAOYSA-N 0.000 description 1
- QIEVIJCOPMNTRU-UHFFFAOYSA-N 2-chloro-6-(N-hydroxy-C-nonylcarbonimidoyl)-4-octan-2-ylphenol Chemical compound C(CCCCCCCC)C(C1=C(C(=CC(=C1)C(C)CCCCCC)Cl)O)=NO QIEVIJCOPMNTRU-UHFFFAOYSA-N 0.000 description 1
- NYOTVCJPZLYUAK-UHFFFAOYSA-N 4-dodecan-2-yl-2-(C-ethyl-N-hydroxycarbonimidoyl)phenol Chemical compound C(C)C(C1=C(C=CC(=C1)C(C)CCCCCCCCCC)O)=NO NYOTVCJPZLYUAK-UHFFFAOYSA-N 0.000 description 1
- TXCHINUMZMMHRD-UHFFFAOYSA-N 4-dodecan-2-yl-2-(N-hydroxy-C-phenylcarbonimidoyl)phenol Chemical compound OC1=C(C(C2=CC=CC=C2)=NO)C=C(C=C1)C(C)CCCCCCCCCC TXCHINUMZMMHRD-UHFFFAOYSA-N 0.000 description 1
- CILYKUDMVIRMGY-UHFFFAOYSA-N 4-dodecyl-2-(N-hydroxy-C-phenylcarbonimidoyl)phenol Chemical compound CCCCCCCCCCCCC1=CC=C(O)C(C(=NO)C=2C=CC=CC=2)=C1 CILYKUDMVIRMGY-UHFFFAOYSA-N 0.000 description 1
- RDHDDAQHIKGTIH-UHFFFAOYSA-N 4-heptan-2-yl-2-(C-heptyl-N-hydroxycarbonimidoyl)phenol Chemical compound C(CCCCCC)C(C1=C(C=CC(=C1)C(C)CCCCC)O)=NO RDHDDAQHIKGTIH-UHFFFAOYSA-N 0.000 description 1
- DLRBAUCIXXQLOT-UHFFFAOYSA-N 4-heptan-2-yl-2-(N-hydroxy-C-methylcarbonimidoyl)phenol Chemical compound CC(C1=C(C=CC(=C1)C(C)CCCCC)O)=NO DLRBAUCIXXQLOT-UHFFFAOYSA-N 0.000 description 1
- XTJPIJQKWONHIX-UHFFFAOYSA-N 4-heptan-2-yl-2-(N-hydroxy-C-nonylcarbonimidoyl)phenol Chemical compound C(CCCCCCCC)C(C1=C(C=CC(=C1)C(C)CCCCC)O)=NO XTJPIJQKWONHIX-UHFFFAOYSA-N 0.000 description 1
- XJABWGHSJLRCCU-UHFFFAOYSA-N 4-hexan-2-yl-2-(N-hydroxy-C-undecylcarbonimidoyl)phenol Chemical compound C(CCCCCCCCCC)C(C1=C(C=CC(=C1)C(C)CCCC)O)=NO XJABWGHSJLRCCU-UHFFFAOYSA-N 0.000 description 1
- RCEAKQYSPGVKEX-UHFFFAOYSA-N 5,8-diethyl-7-hydroxydodecan-6-one Chemical compound CCCCC(CC)C(O)C(=O)C(CC)CCCC RCEAKQYSPGVKEX-UHFFFAOYSA-N 0.000 description 1
- ZGBVVXQGIYLOFZ-UHFFFAOYSA-N 5-dodecoxy-2-(N-hydroxy-C-phenylcarbonimidoyl)phenol Chemical compound C(CCCCCCCCCCC)OC1=CC(=C(C(C2=CC=CC=C2)=NO)C=C1)O ZGBVVXQGIYLOFZ-UHFFFAOYSA-N 0.000 description 1
- PLMNNCSEGVDRMV-UHFFFAOYSA-N 6,9-diethyl-8-hydroxyiminotetradecan-7-ol Chemical compound C(C)C(CCCCC)C(C(C(CCCCC)CC)O)=NO PLMNNCSEGVDRMV-UHFFFAOYSA-N 0.000 description 1
- ATRRKUHOCOJYRX-UHFFFAOYSA-N Ammonium bicarbonate Chemical compound [NH4+].OC([O-])=O ATRRKUHOCOJYRX-UHFFFAOYSA-N 0.000 description 1
- ZNSMNVMLTJELDZ-UHFFFAOYSA-N Bis(2-chloroethyl)ether Chemical compound ClCCOCCCl ZNSMNVMLTJELDZ-UHFFFAOYSA-N 0.000 description 1
- DDUYHDMBLGZSPD-UHFFFAOYSA-N C(C)(CCCCCC)C=1C=CC(=C(C(C2=CC=CC=C2)=NO)C1)O Chemical compound C(C)(CCCCCC)C=1C=CC(=C(C(C2=CC=CC=C2)=NO)C1)O DDUYHDMBLGZSPD-UHFFFAOYSA-N 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 description 1
- 229910002651 NO3 Inorganic materials 0.000 description 1
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 1
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- 125000002877 alkyl aryl group Chemical group 0.000 description 1
- BVCZEBOGSOYJJT-UHFFFAOYSA-N ammonium carbamate Chemical compound [NH4+].NC([O-])=O BVCZEBOGSOYJJT-UHFFFAOYSA-N 0.000 description 1
- 239000001099 ammonium carbonate Substances 0.000 description 1
- 235000012501 ammonium carbonate Nutrition 0.000 description 1
- 150000003868 ammonium compounds Chemical class 0.000 description 1
- BFNBIHQBYMNNAN-UHFFFAOYSA-N ammonium sulfate Chemical compound N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 description 1
- 229910052921 ammonium sulfate Inorganic materials 0.000 description 1
- 235000011130 ammonium sulphate Nutrition 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- 238000011001 backwashing Methods 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- KXDHJXZQYSOELW-UHFFFAOYSA-N carbonic acid monoamide Natural products NC(O)=O KXDHJXZQYSOELW-UHFFFAOYSA-N 0.000 description 1
- 125000001309 chloro group Chemical group Cl* 0.000 description 1
- OBWXQDHWLMJOOD-UHFFFAOYSA-H cobalt(2+);dicarbonate;dihydroxide;hydrate Chemical compound O.[OH-].[OH-].[Co+2].[Co+2].[Co+2].[O-]C([O-])=O.[O-]C([O-])=O OBWXQDHWLMJOOD-UHFFFAOYSA-H 0.000 description 1
- 229910000001 cobalt(II) carbonate Inorganic materials 0.000 description 1
- 230000003750 conditioning effect Effects 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 125000004093 cyano group Chemical group *C#N 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 239000012527 feed solution Substances 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 230000036571 hydration Effects 0.000 description 1
- 238000006703 hydration reaction Methods 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 229910052750 molybdenum Inorganic materials 0.000 description 1
- 239000011733 molybdenum Substances 0.000 description 1
- 125000003136 n-heptyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 229910000008 nickel(II) carbonate Inorganic materials 0.000 description 1
- 229910021508 nickel(II) hydroxide Inorganic materials 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 238000007873 sieving Methods 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 229910021653 sulphate ion Inorganic materials 0.000 description 1
- 229910052720 vanadium Inorganic materials 0.000 description 1
- GPPXJZIENCGNKB-UHFFFAOYSA-N vanadium Chemical compound [V]#[V] GPPXJZIENCGNKB-UHFFFAOYSA-N 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- 150000003738 xylenes Chemical class 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D11/00—Solvent extraction
- B01D11/04—Solvent extraction of solutions which are liquid
- B01D11/0492—Applications, solvents used
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01G—COMPOUNDS CONTAINING METALS NOT COVERED BY SUBCLASSES C01D OR C01F
- C01G53/00—Compounds of nickel
- C01G53/01—Preparation or separation involving a liquid-liquid extraction, an adsorption or an ion-exchange
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22B—PRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
- C22B3/00—Extraction of metal compounds from ores or concentrates by wet processes
- C22B3/20—Treatment or purification of solutions, e.g. obtained by leaching
- C22B3/26—Treatment or purification of solutions, e.g. obtained by leaching by liquid-liquid extraction using organic compounds
- C22B3/30—Oximes
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P10/00—Technologies related to metal processing
- Y02P10/20—Recycling
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Environmental & Geological Engineering (AREA)
- Materials Engineering (AREA)
- General Life Sciences & Earth Sciences (AREA)
- Geochemistry & Mineralogy (AREA)
- Geology (AREA)
- Inorganic Chemistry (AREA)
- Manufacturing & Machinery (AREA)
- Life Sciences & Earth Sciences (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Manufacture And Refinement Of Metals (AREA)
- Extraction Or Liquid Replacement (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB6095071A GB1411545A (en) | 1971-12-31 | 1971-12-31 | Separation of metal values by liquid-liquid extraction |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| NO131082B true NO131082B (enrdf_load_stackoverflow) | 1974-12-23 |
| NO131082C NO131082C (enrdf_load_stackoverflow) | 1975-04-02 |
Family
ID=10486359
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO4831/72A NO131082C (enrdf_load_stackoverflow) | 1971-12-31 | 1972-12-29 |
Country Status (13)
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1497535A (en) * | 1973-12-13 | 1978-01-12 | Matthey Rustenburg Refines | Separation of palladium |
| CA1185406A (en) * | 1982-01-25 | 1985-04-16 | Gary A. Kordosky | Solvent extraction |
| ID827B (id) * | 1987-05-20 | 1996-07-25 | Meq Nickel Pty Ltd | Pemisahan dan perolehan kembali nikel dan kobal dalam sistem-sistem amoniak |
| CA1338345C (en) * | 1988-06-14 | 1996-05-28 | Gary A. Kordosky | Nickel extraction with oxime extractants |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5248091A (en) * | 1975-10-15 | 1977-04-16 | Keru Kk | Connector |
-
1971
- 1971-12-31 GB GB6095071A patent/GB1411545A/en not_active Expired
-
1972
- 1972-11-27 CA CA157,594A patent/CA995012A/en not_active Expired
- 1972-12-22 IT IT33532/72A patent/IT972874B/it active
- 1972-12-28 ZA ZA729134A patent/ZA729134B/xx unknown
- 1972-12-29 AU AU50622/72A patent/AU470827B2/en not_active Expired
- 1972-12-29 FR FR7246970A patent/FR2166192B1/fr not_active Expired
- 1972-12-29 BR BR9257/72A patent/BR7209257D0/pt unknown
- 1972-12-29 SE SE7217233A patent/SE389513B/xx unknown
- 1972-12-29 JP JP734237A patent/JPS5522537B2/ja not_active Expired
- 1972-12-29 NO NO4831/72A patent/NO131082C/no unknown
- 1972-12-29 FI FI3711/72A patent/FI56554C/fi active
- 1972-12-29 DE DE2264089A patent/DE2264089A1/de not_active Withdrawn
- 1972-12-29 PH PH14218A patent/PH10172A/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| NO131082C (enrdf_load_stackoverflow) | 1975-04-02 |
| JPS4879122A (enrdf_load_stackoverflow) | 1973-10-24 |
| PH10172A (en) | 1976-09-15 |
| ZA729134B (en) | 1973-09-26 |
| DE2264089A1 (de) | 1973-07-12 |
| FR2166192A1 (enrdf_load_stackoverflow) | 1973-08-10 |
| JPS5522537B2 (enrdf_load_stackoverflow) | 1980-06-17 |
| FI56554B (fi) | 1979-10-31 |
| FR2166192B1 (enrdf_load_stackoverflow) | 1976-08-27 |
| FI56554C (fi) | 1980-02-11 |
| AU470827B2 (en) | 1974-07-04 |
| GB1411545A (en) | 1975-10-29 |
| CA995012A (en) | 1976-08-17 |
| BR7209257D0 (pt) | 1973-09-13 |
| IT972874B (it) | 1974-05-31 |
| SE389513B (sv) | 1976-11-08 |
| AU5062272A (en) | 1974-07-04 |
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